@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_head
{
this:
np:hasAssertion
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_assertion
;
np:hasProvenance
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_provenance
;
np:hasPublicationInfo
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_assertion
a
np:Assertion
.
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_provenance
a
np:Provenance
.
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_assertion
{
miriam-gene:338
a
ncit:C16612
.
lld:C3272363
a
ncit:C7057
.
dgn-gda:DGNda03b81703445611d7935fee641c5be1
sio:SIO_000628
miriam-gene:338
,
lld:C3272363
;
a
sio:SIO_001121
.
}
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_provenance
{
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_assertion
dcterms:description
"[The apolipoprotein B gene (APOB) polymorphisms may influence levels of ApoB and risk of ischemic stroke, but whether they are associated with risk of ischemic cerebral infarction (CI) with family history (CIFH) or not is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:19934556
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP898815.RARRkJtdBjx6wWYiOJ09uNpTvIHp5tI6zPjdINgrxc4zk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:12+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}